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A "DIRECT-COLORING" THIOCHOLINE METHOD FOR CHOLINESTERASES.
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The active site of esterases.
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J Physiol. 1973 May;230(3):673-88
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J Cell Biol. 1969 Jun;41(3):665-85
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"Disjunction" of frog neuromuscular synapses by treatment with proteolytic enzymes.
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J Physiol. 1975 Oct;251(2):465-82
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Periodate-lysine-paraformaldehyde fixative. A new fixation for immunoelectron microscopy.
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Sizes of end plate compartments, densities of acetylcholine receptor and other quantitative aspects of neuromuscular transmission.
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Localization of acetylcholine receptor by 125I-labeled alpha-bungarotoxin binding at mouse motor endplates.
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Quantitative assay of esterases in end plates of mouse diaphragm by electron microscope autoradiography.
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Sensitivity in electron microscope autoradiography. I. The effect of radiation dose.
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Quantitation of junctional and extrajunctional acetylcholine receptors by electron microscope autoradiography after 125I-alpha-bungarotoxin binding at mouse neuromuscular junctions.
J Cell Biol. 1976 Apr;69(1):144-58
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The density of cholinergic receptors at the endplate postsynaptic membrane: ultrastructural studies in two mammalian species.
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Electron microscope radioautography as a quantitative tool in enzyme cytochemistry. II. The distribution of DFP-reactive sties at motor endplates of a vertebrate twitch muscle.
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Electron microscopic localization of acetylcholinesterase and nonspecific cholinesterase at the neuromuscular junction by the gold-thiocholine and gold-thiolacetic acid methods.
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In vivo studies on fast and slow muscle fibers in cat extraocular muscles.
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Number and location of acetylcholinesterase molecules at motor endplates of the mouse.
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Dealkylation studies on inhibited acetylcholinesterase.
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Neuromuscular junctions in a fast-contracting fish muscle.
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